AR114941A1 - Derivados de sulfonilurea - Google Patents

Derivados de sulfonilurea

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Publication number
AR114941A1
AR114941A1 ARP180103694A ARP180103694A AR114941A1 AR 114941 A1 AR114941 A1 AR 114941A1 AR P180103694 A ARP180103694 A AR P180103694A AR P180103694 A ARP180103694 A AR P180103694A AR 114941 A1 AR114941 A1 AR 114941A1
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AR
Argentina
Prior art keywords
alkyl
halo
optionally substituted
cycloalkyl
haloalkyl
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ARP180103694A
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English (en)
Inventor
Mark G Bock
Alan Paul Watt
David Harrison
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Nodthera Ltd
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Application filed by Nodthera Ltd filed Critical Nodthera Ltd
Publication of AR114941A1 publication Critical patent/AR114941A1/es

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    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4151,2-Diazoles
    • A61K31/41551,2-Diazoles non condensed and containing further heterocyclic rings
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    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/42Oxazoles
    • A61K31/422Oxazoles not condensed and containing further heterocyclic rings
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    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445Non condensed piperidines, e.g. piperocaine
    • A61K31/4523Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A61K31/454Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
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    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/10Anti-acne agents
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    • A61P25/00Drugs for disorders of the nervous system
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    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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    • C07D249/101,2,4-Triazoles; Hydrogenated 1,2,4-triazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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Abstract

La presente descripción se refiere a compuestos de la fórmula (1), y a sus sales farmacéuticamente aceptables, composiciones farmacéuticas, métodos de uso y métodos para su preparación. Los compuestos revelados en la presente son de utilidad para inhibir la maduración de las citoquinas de la familia IL-1 por inhibición de inflamasomas y se pueden usar en el tratamiento de trastornos en los que está implicada la actividad de inflamasomas, tales como enfermedades inflamatorias, autoinflamatorias y autoinmunes y cánceres. Reivindicación 1: Un compuesto de la fórmula (1), o uno de sus profármacos, solvatos o sales farmacéuticamente aceptables, en donde: R¹ es cicloalquilo C₃₋₁₆ o arilo C₅₋₁₀, en donde el cicloalquilo C₃₋₈ monocíclico, cicloalquilo policíclico o arilo C₅₋₆ está opcionalmente sustituido con uno o más R¹S; en donde cada R¹S es, de modo independiente, alquilo C₁₋₆, haloalquilo C₁₋₆, alcoxi C₁₋₆, haloalcoxi C₁₋₆ o halo; R² es -(CX²X²)ₙ-R²S, en donde n es 0, 1 ó 2 y cada X² es, de modo independiente, H, alquilo C₁₋₆, alquenilo C₂₋₆ o alquinilo C₂₋₆, en donde el alquilo C₁₋₆, alquenilo C₂₋₆ o alquinilo C₂₋₆ está opcionalmente sustituido con uno o más halo, -CN, -OH, -O(alquilo C₁₋₆), -NH₂, -NH(alquilo C₁₋₆), -N(alquilo C₁₋₆)₂ u oxo; R²S es heterocicloalquilo de 4 a 8 miembros opcionalmente sustituido con uno o más alquilo C₁₋₆, alquenilo C₂₋₆, alquinilo C₂₋₆, haloalquilo C₁₋₆, halo, -CN, -OH, -O(alquilo C₁₋₆), -NH₂, -NH(alquilo C₁₋₆), -N(alquilo C₁₋₆)₂ u oxo; y R³ es heterocicloalquilo de 7 a 12 miembros o heteroarilo de 5 ó 6 miembros opcionalmente sustituido con uno o más R³S, en donde cada R³S es, de modo independiente, alquilo C₁₋₆, haloalquilo C₁₋₆, cicloalquilo C₃₋₈, halo o heterocicloalquilo C₃₋₈, en donde el alquilo C₁₋₆, haloalquilo C₁₋₆, cicloalquilo C₃₋₈ o heterocicloalquilo C₃₋₈ está opcionalmente sustituido con -O(alquilo C₁₋₆), -N(alquilo C₁₋₆)₂, halo o -CN.
ARP180103694A 2017-12-18 2018-12-18 Derivados de sulfonilurea AR114941A1 (es)

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KR (1) KR20200101423A (es)
CN (1) CN111954670A (es)
AR (1) AR114941A1 (es)
AU (1) AU2018391675B2 (es)
BR (1) BR112020011779A2 (es)
CA (1) CA3084694A1 (es)
EA (1) EA202091512A1 (es)
GB (1) GB201721185D0 (es)
IL (1) IL275058A (es)
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